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ICON (Lenexa, KS)

9755 Ridge Dr. Lenexa, KS 66219

Research Site Introduction:

Headquartered in Dublin, Ireland, ICON is the world's largest and most comprehensive clinical research organization. Our company's nearly 38,000 employees at 127 locations in 46 countries work to help clients accelerate the development of drugs and devices that save lives and improve quality of life for patients globally. 

Research Site Description:

ICON's full-service clinic in Lenexa, Kansas, is a state-of-the-art research center, located near metropolitan Kansas City. Our experienced team of physicians, clinic staff and support staff are dedicated to making our participants' time in our facility as positive and comfortable as possible. With a 114-bed capacity, our Lenexa facility features spacious common areas for interacting with other study participants, big-screen TVs, comfortable seating, a pool table, gaming systems, foosball, a dart board, DVDs, satellite TV, computers and more. We also offer WiFi access for those interested in bringing their own electronic devices.

Patient Demographics:

Our Lenexa clinic regularly conducts a Phase I and II studies and has extensive experience in conducting healthy volunteer studies, first-in-human studies, bioequivalence studies, bioavailability studies, drug-drug interacion studies, human abuse potential, human abuse liability studies and many more. Along with healthy participants, our studies have delved into investigational medications for those suffering from conditions such as diabetes, hypertension, dermatology issues, epilepsy and others.

Additional Information:

Thinking of extending your stay in the Kansas City area after your study ends? Whether you want to scope out the nightlife at the Power & Light District, Westport or The Crossroads Distric, do some shopping on the famed Country Club Plaza, or enjoy some delicious, world-famous barbecue at Joe's Kansas City, we've got plenty of options. Don't forget that Kansas City is also home to the Royals, Chiefs, Sporting Kansas City, the Kansas Speedway and so much more. Find out more at VisitKC.com. 

Contact Information:

ICON (Lenexa, KS) 9755 Ridge Dr. Lenexa, KS 66219

Phone: 913-285-5700 Web: ICONstudies.com/Lenexa

Active Studies:

There are no active studies for this clinic.

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Our Locations

Strategically positioned to serve a diverse population., our vast experience and excellence in clinical research allow us to custom design a plan that works best for you in any of our 32 locations..

“Especially when I have large studies that need large numbers of subjects enrolled quickly and with quality and good investigator oversight, I always involve AMR sites.”

“AMR sites were pivotal to the success of our seasonal vaccine program.  All AMR sites met and exceeded enrollment expectations.  The variety of experience and expertise among AMR sites has helped us enroll a broad therapeutic range of clinical trials.”

“I’ve been doing this job for 18 years and have met with literally thousands of customers.  After all that, today was the single best customer visit I’ve ever had,  I had high expectations going into the meeting, but you blew my expectations away.  The combination of your incredible capacity and performance in clinical trials combined with your hospitality made this the absolute perfect day.”

Chicago, IL

Amr chicago brings together physicians in multiple specialties who offer clinical trial services to the highest standards of good clinical practice..

AMR Chicago was formerly known as Affinity Health.

AMR Daphne is Located in a professional medical office building attached to the Sleep & Cardiovascular health practice run by Dr. Ledet.

Founded in 2022 27+ clinical trials Phase I, II, III, and IV

Dearborn, MI

Amr dearborn is our newest clinical research center conveniently located in dearborn, michigan that will primarily focus on cardiology clinical trials as well as hypercholesterolemia, obesity, and vaccines..

Founded in 2023 Phase I, II, III, and IV Arabic Also Spoken

El Dorado, KS

Amr el dorado is located in the susan b. allen memorial hospital..

Founded in 1991 1,400+ clinical trials Phase I, II, III, and IV

AMR El Dorado was formerly known as Heartland Research Associates.

Fort Myers, FL

Amr fort myers is across the street from the newest hospital in fort myers..

Founded in 1978 700+ clinical trials Phase I, II, III, and IV

AMR Fort Myers was formerly known as Clinical Physiology Associates.

Kansas City, MO

Amr kansas city has conducted more trials since 1986 and owns a database of more than 33,000 volunteers..

Founded in 1986 800+ clinical trials Phase I, II, III, and IV

AMR Kansas City was formerly known as The Center for Pharmaceutical Research.

Kansas City Oncology, KS

Amr kansas city oncology.

75 clinical trials

5 Oncologists and 10 oncology nurse practitioners

Knoxville, TN

Amr knoxville is located in an academic medical center with state-of-the-art capabilities..

Founded in 1985 1,900+ clinical trials Phase I, II, III, and IV

AMR Knoxville was formerly known as Volunteer Research Group/NOCCR-Knoxville.

Las Vegas, NV

Amr las vegas is located on a medical campus across the street from desert springs hospital..

Founded in 2003 250+ clinical trials Phase I, II, III, and IV

AMR Las Vegas was formerly known as Clinical Research Consortium in Las Vegas.

Founded in 2000 670+ clinical trials Phase I, II, III, and IV

AMR Layton was formerly known as Pharmaceutical Research Organization.

Lexington, KY

Amr lexington was kentucky’s first independent clinical drug research facility..

Founded in 1991 600+ clinical trials Phase I, II, III, and IV

AMR Lexington was formerly known as Central Kentucky Research Associates.

AMR Miami in Coral Gables, Florida has recently invested in a PBMC lab, which became functional in May 2018.

Founded in 1982 813+ clinical trials Phase I, II, III, and IV

AMR Miami was formerly known as Clinical Research of South Florida.

AMR Mobile was the first free-standing multispecialty research site in the state of Alabama.

Founded in 1987 850+ clinical trials Phase I, II, III, and IV

AMR Mobile was formerly known as Coastal Clinical Research.

New Orleans, LA

Amr new orleans is a dedicated research clinic located in the mid-city area on canal street..

Founded in 1985 900+ clinical trials Phase I, II, III, and IV

AMR New Orleans was formerly known as NOCCR.

AMR Newton is connected to the Axtell Clinic, which has provided care for over 100 years.

AMR Newton was formerly known as Heartland Research Associates.

Norfolk, VA

Amr norfolk is located on the campus of eastern virginia medical complex..

Founded in 1983 700+ clinical trials Phase I

AMR Norfolk was formerly known as Clinical Research Associates of Tidewater.

AMR Norman is located in the heart of the Midwest – just 30 minutes from Oklahoma City in Norman, Oklahoma.

Phoenix, AZ

Amr phoenix is located in the medical office building on the campus of tempe st. luke’s hospital..

Founded in 2011 250+ clinical trials Phase I, II, III, and IV

AMR Phoenix was formerly known as Clinical Research Consortium.

Salt Lake City, UT

AMR Utah was formerly known as Pharmaceutical Research Organization.

Wichita - East, KS

Amr wichita – east is within family medicine east, a private practice clinic..

AMR Wichita-East was formerly known as Heartland Research Associates.

Wichita - West, KS

Amr wichita.

AMR Wichita-West was formerly known as Heartland Research Associates.

Find Your Nearest AMR Center

AMR Chicago aims to deliver quality healthcare with a patient-centered approach. We provide variety of medical services & clinical research trials with compassion, while ensuring exceptional patient care and safety.

2001 Midwest Road, Suite 305 Oak Brook, IL 60523

630-491-1900 [email protected]

AMR Daphne is Located in a professional medical office building attached to the Sleep & Cardiovascular health practice run by Dr. Ledet, who also serves as Medical Director at Southeast Regional Center for Sleep/Wake Disorders since its inception in the early 1990s. His focus of healthcare is on sleep and cholesterol disorders to prevent and manage cardiovascular disease, which includes caring for risk factors such as insulin resistance. Our full-time research team includes clinical research coordinators, back-up coordinators, patient recruiters, lab coordinator, data entry coordinator, regulatory specialist, and administrative staff. We provide our community with innovative treatments and the highest quality of care throughout each clinical research trial.

7101 Hwy 90, Suite 102 Daphne, AL 36526

251-901-2111 [email protected]

AMR currently has two investigators to conduct clinical research trials in the Dearborn community, Dr. Elias H. Kassab and Dr. Ashok K. Kondur. Dr. Kassab serves as Principal Investigator. Dr. Kassab completed his graduate training and fellowship in cardiology throughout Michigan after completing his education at Universite Libre de Bruxelles, Brussels, Belgium in 1982. In addition to clinical research, his experience includes Cardiology, Endovascular and Vascular Management. Dr. Kondur is the Sub Investigator for the site. Dr. Kondur is board-certified in PET imaging, Nuclear Medicine, Vascular Medicine and Coronary, Peripheral, Structural and Endovascular Interventions. Both Dr. Kondur and Dr. Kassab will focus primarily on Cardiology clinical trials as well as conducting trials focused on Hypercholesterolemia, Obesity, and Vaccines.

5250 Auto Club Drive, Suite 310B Dearborn, Michigan  48126

251-901-2111 [email protected]

AMR Heartland Research Associates – El Dorado, Kansas (previously located in Augusta, Kansas) is located in the Susan B. Allen Memorial Hospital.  It has conducted more than 75 Phase I–IV pharmaceutical and device trials since opening in 2010.  Three family practice clinics in the Augusta / El Dorado and neighboring communities are owned by the center’s research investigator.  Access to these subjects makes enrollment efforts highly successful.

• General Manager: Jill Hiebert
• Managing Principal Investigators: Thomas Klein, MD, FAAFP, CPI; Terry Klein, MD, DABFM, CPA; Tracy Klein, MD, DABFM, CPI, Terry Poling, MD, DABFM, FAAFP, CPI
• Founded in 1991
• Conducted 1,400+ clinical trials
• Phase I, II, III, and IV trials
• Limited overnight stay capabilities (expanded phase I capabilities coming soon)

Specialties:

• Infant Vaccines
• Adult Vaccines
• Maternal Health

700 W. Central, Suite 101 El Dorado, KS 67042 316-600-5127

Pharmaceutical Research Organization, now AMR Utah,  conducts and manages the day-to-day clinical research trial at the investigative site level under the direction of the principal investigator. While we manage a wide-range of trial types, AMR Utah has expertise and a focus in pediatric vaccines.

• Site Manager: Shelly Searle
• Business Development & Community Relations: Luke Johnson
• Founded in 2000
• Conducted 670+ clinical trials
• Mainly Phase II, III, and IV clinical research protocols
• Dermatology
• Family Practice
• Gastroenterology
• Internal Medicine
• Obstetrics & Gynecology
• Ophthalmology
• Pediatric Dentistry

1492 West Antelope Drive, Suite 209 Layton, Utah 84041 (801) 294-9911

Pharmaceutical Research Organization, now AMR Layton,  conducts and manages the day-to-day clinical research trial at the investigative site level under the direction of the principal investigator. While we manage a wide-range of trial types, AMR Layton has expertise and a focus in pediatric vaccines.

• Site Manager: Curtis Thomas
• Business Developmen: Luke Johnson

2132 N 1700 W, Suite 200 Layton, UT 84041 (801) 679-4153

AMR Fort Myers (aka Clinical Physiology Associates and the Clinical Study Center), Fort Myers, Florida has conducted more than 800 Phase I–IV clinical research trials since 1978. The center is located across the street from the newest hospital in Fort Myers, which recently completed a $350 million expansion. Led by principal investigator, Dr. Pedro Ylisisatigui, AMR Fort Myers has developed research relationships with local doctors focusing on internal medicine, women’s health, dermatology, endocrinology and pain management. The Ft. Myers location has a long-standing research relationship with Premier Women’s Care, the largest OB/GYN group in the area and has completed more than 130 women’s health studies in the past 15 years. The center has two beds for overnight studies.

• General Manager: Ken Aschom
• Founded in 1978
• Conducted 800+ clinical trials
• Limited overnight stay capabilities
• Women’s and Men’s Health
• Musculoskeletal
• Endocrinology
• Pain Management

13670 Metropolis Ave. Suite 105 Fort Myers, FL 33912 239-936-4421 239-936-2865 fax

AMR Volunteer Research Group for Clinical Research(Knoxville, TN) and AMR New Orleans Center for Clinical Research(New Orleans, LA) operate as three distinct units;

• 60-bed inpatient PK unit in Knoxville at the University of Tennessee Medical Center
• an outpatient unit in Knoxville
• the original facility, which is now an outpatient unit in New Orleans

These centers have conducted more than 1,900 Phase I–IV trials since opening in 1991. The inpatient unit employs 60 full-time staff and conducts a variety of trials including NHV, SAD/MAD, FIH, special population trials including renal, hepatic, diabetic, obese and elderly among others, as well as hybrid studies starting in HNV and bridging into patient populations such as Alzheimer’s disease, Parkinson’s disease, COPD, ALS as well as cancer subjects. It also conducts inpatient vaccine and smoking-related trials. The site focuses on complex studies which lend themselves to being performed in a level-one trauma facility with 24/7 rapid-response code team coverage. Located in an academic medical center, the site has relationships with more than 800 physicians, unique state-of-the-art imaging, diagnostic and laboratory capabilities.

The outpatient units in Knoxville and New Orleans function as Phases II-IV research sites conducting efficacy trials from vaccine, obesity, migraine, diabetes and hypertension to women’s and men’s health, COPD and generally all internal medicine-related indications. The New Orleans location has been in operation since the early 1980s and was a base of operation until Hurricane Katrina forced relocation in 2005. The Knoxville location has been in operation since 1998.

Staff has an average longevity of 15 years. The site has an exemplary track record of compliancy, having successfully passed the last five FDA inspections in which NOCCR was found to be in full compliance with FDA rules and regulations.

• General Manager: Nyda Brook
• Founded in 1985
• Conducted 1,900+ clinical trials
• Cardiovascular
• Neuropsychology
• Complex Inpatient Trials
• Sleep Disorders
• Elderly PK and Healthy Phase I
• Tobacco Related

1924 Alcoa Hwy 4th & 5th Floors North Tower Knoxville, TN 37920

801 North Weisgarber Rd. Suite 100 Knoxville, TN 37909 865-305-9100 865-305-8381 fax

AMR – Lexington, Central Kentucky Research Associates, in Lexington, Kentucky has conducted 608 Phase I–IV trials since opening in 1991.  This was Kentucky’s first independent clinical drug research facility and is housed in a 17,000 square foot facility that contains both an outpatient Phase II-IV clinic and an inpatient 23-bed Phase I and overnight unit.

AMR Lexington is fully staffed and has educated coordinator staff who are supported by a strong team of professionals who assist with regulatory, operations, data management, and quality assurance. The location also has trained PRN employees who can be called upon to assist in the conduct of overnight and Phase I trials. Staff at the Lexington location have 75-plus years of combined clinical research experience.

• General Manager: Ginger Switzer
• Conducted >600 clinical trials
• Full service phase I unit with 25 beds
• Tobacco and Vape
• Hypertension

3475 Richmond Rd. 3rd Floor Lexington, KY 40509 859-264-8999

AMR Clinical Research Associates of Tidewater/(CRAT) in Norfolk, Virginia was founded in 1983 and has conducted 700 Phase I–IV trials.  The center is conveniently located on the campus of Eastern Virginia Medical Complex, home to the area’s only Level One Trauma Center; Children’s Hospital of the King’s Daughters and Eastern Virginia Medical School.  The center has four beds, which allows for the conduct of overnight studies. The Norfolk location is currently investing in a PBMC laboratory, which opened in 2018.

• Founded in 1983
• Conducted more than 600 clinical trials
• Primary specialties include: vaccines, women’s health, men’s health, osteoarthritis, smoking/smoking cessation, obesity, neurology (DPN, PHN, migraines) and dermatology
• Women’s & men’s health
• Tobacco/smoking cessation

6161 Kempsville Circle Suite 225 Norfolk, VA 23502 757-627-7446 757-624-1121 fax

Founded in Coral Gables, Florida in 1982, AMR Miami conducted 842 Phase I-IV clinical trials in a wide range of therapeutic areas.  This facility has two beds for overnight studies and has access to a 16-bed fully staffed Phase I center. In addition, AMR Miami has access to two PBMC labs which are actively in use. AMR Miami has strong ties with the local community and its diverse population. This site also maintains a strategic partnership with PrimeHealth Physicians, a 40-provider primary care practice in the Miami/Coral Gables area; a key partner for the sourcing of trial participants.

• Healthy Blood Draw
• Rheumatology/Musculoskeletal

370 Minorca Ave Coral Gables, Florida 33134 305-445-5637 [email protected]

Founded in 1987, AMR Coastal Clinical Research was the first free-standing multispecialty research site in the state of Alabama. To date, the Mobile location has conducted more than 851 biotech and pharmaceutical-sponsored clinical research trials in Phases I-IV.

The Mobile location features a unique mixture of seasoned Investigators with different board-certified specialties that has resulted in stability and steady growth during their 30+ years in business. Mobile’s database includes subjects from the local community, surrounding areas, and parts of Mississippi, Florida and Louisiana. The Mobile location is also on the grounds of Springhill Medical Center in Mobile, AL, with access to all of their diagnostic and medical equipment. The site has an overnight capacity of 8 beds.

This location is the largest dedicated research site in Mobile with competition insignificant to new business and the growth of its database. The Investigator’s reputable private practices are separate from CCR and provide another avenue for recruiting quality subjects.

• Orthopedics
• Smoking Cessation

100 Memorial Hospital Drive Annex Building, Suite 3-B Mobile, AL 36608 251-414-1984 [email protected]

New Orleans

NOCCR-New Orleans was established in 1985 and has conducted over 900 trials in Phase I-IV. NOCCR is a dedicated research clinic located in the Mid-City area on Canal Street. The unit has extensive experience in tobacco trials, women’s and men’s health, vaccines, diabetes, hypertension as well as other indications. Being located close to Tulane, Ochsner and University Medical Centers allows NOCCR to have remote access to DEXA, Interventional Radiology, EEGs, Treadmills, etc. The unit has a catchment area of approximately 1.3 million people and maintain a subject database of over 45,000 subjects.

• Healthy volunteer
• Rheumatology / musculoskeletal
• Internal medicine
• Smoking cessation

2820 Canal Street New Orleans, LA 70119 504-821-8158 [email protected]

AMR Las Vegas, formerly Clinical Research Consortium, was founded in 2003 and has conducted 250+ Phase I-IV trials. The Las Vegas, NV location has 8 overnight beds and has recently doubled the size of the recruitment staff to six employees. Located across the street from Desert Springs Hospital, AMR Las Vegas has strong ties with the local community and its diverse population. The center has an active daily pre-screening clinic to pre-identify potential subjects for various studies that are ongoing and upcoming.

• Founded in 2003
• Conducted >250 clinical trials
• Full-service phase 1 unit with 8 beds
• Primary specialties include: vaccines, respiratory/pulmonary, musculoskeletal, immunology, genitourinary, endocrine/metabolic, chronic pain, devices.
• Tobacco/Smoking Cessation
• Healthy Volunteer

2110 E Flamingo Rd Suite 308 Las Vegas, NV 89119 To reach the receptionist, please call: 702-597-9825 If you are interested in participating in a study, please call: 702-545-6840

702-597-1596 fax

AMR Phoenix, formerly Clinical Research Consortium, is a dedicated multispecialty clinical research center that has been in operation since 2011 and has conducted 250+ Phase I-IV Clinical Trials. Dr. Corey Anderson, Principal Investigator, has over 18 years of clinical trials experience across an ever-expanding array of therapeutic areas and indications. AMR Phoenix is conveniently located in the medical office building on the campus of Tempe St. Luke’s Hospital and has 8 overnight beds. The center has an active daily pre-screening clinic to pre-identify potential subjects for various studies that are ongoing and upcoming.

• Founded in 2011
• Primary specialties include: vaccines, respiratory/pulmonary, musculoskeletal, immunology, genitourinary, endocrine/metabolic, chronic pain, device, dermatology.

1492 S. Mill Ave. Suite 312 Tempe, AZ 85281 602-759-7559

AMR’s Kansas City, Missouri location, the Center for Pharmaceutical Research, has conducted more than 730 Phase I–IV trials since 1986 and owns a database of more than 29,000 volunteers. Staff includes more than 33 full-time employees with 274-plus years of combined research experience.  The Kansas City center is located on the Joint Commission-accredited St. Joseph Medical Center campus and works with a major imaging center to include access to a 3.0 Tesla MRI.

Since 2005, the Kansas City team has conducted more than 90 vaccine trials, including 12 Phase I vaccine studies and numerous complex vaccine trials including PBMC samples, with Institutional Biosafety Committees, government contracts, complex vaccine compounding, and Biosafety Level -2 certification.  Kansas City has successfully passed four FDA audits, not for cause, with no findings or 483s. In addition, this ocation has recently finalized a relationship that will allow access to 32 hospital beds for overnight studies.

• General Manager: Barbara Bradshaw
• Founded in 1986
• Conducted >730 clinical trials

1010 Carondelet Drive Suite 426 Kansas City, MO 64114 816-943-0770 [email protected]

AMR – Newton has been conducting high-quality clinical research since 2003 as Heartland Research Associates; including more than 375 Phase I–IV pharmaceutical and device trials. Over the years, they have completed two not-for-cause FDA audits of which neither resulted in any findings or any FDA Form 483s being issued.

The Newton location is connected to Axtell Clinic, a large, five-provider owned, family practice medical facility, which has been providing quality medical care to Newton, Kansas and the surrounding communities for more than 100 years.  This creates an excellent partnership between research and practicing medicine in which the subjects have an established history of trust with the center’s investigators. This location employs 22 staff and has six dedicated research exam rooms and 20 overflow exam rooms available.

• General Manager: Shannon Thomas
• Managing Principal Investigators: Richard M. Glover II,MD; Stacy B. Slechta, DO; William R. Beck, MD; Robyn D. Hartvickson, MD; Troy A. Holdeman, MD
• Conducted >1,400 clinical trials
• Adult vaccines
• Infant vaccines and maternal health
• Women’s health

700 Medical Center Drive Suite 110 Newton, KS 67114 316-804-7301

Wichita – East

AMR Heartland Research Associates, Wichita – East has been a leader in clinical research studies since 1991, conducting more than 730 Phase I–IV pharmaceutical and device trials. The center has completed nine FDA audits, not-for cause, of which none resulted in any findings or 483s. The group is located in the well-established Wichita, Kansas area, with its research operation constructed within Family Medicine East, a private practice clinic, which is also owned and operated by primary investigators. The strong and trusting physician/patient relationships aid in successful recruitment, compliance and retention. This location employs 36 staff, has 6 dedicated research exam rooms, 30 overflow exam rooms, and two beds for overnight studies.

• Primary specialties include: vaccines, women’s health, diabetes, osteoarthritis, obesity, dermatology, and gastroenterology

Speciaties:

• Plastic surgery
• Rheumatology
• Alzheimer’s disease
• Intra-articular injections
• Metabolic disorders

1709 S. Rock Road Wichita, KS 67207 316-689-6635

Wichita – West

AMR Heartland Research Associates Wichita – West was established in 2001 and has proudly conducted more than 215 Phase I–IV pharmaceutical and device trials. Recently, the site completed a not-for-cause FDA audit, which did not result in any findings and no FDA Form 483s were issued.  This large database of established patients, who trust in the center’s investigators, makes for quality subjects with verifiable medical histories. This location employs 11 staff, has five dedicated research exam rooms, and 20 overflow exam rooms available.

• General Manager:  Shannon Thomas
• Managing Principal Investigators: Richard Egelhof, MD; William Simon, DO; Paula Worley, MD
• Women’s health
• Alzheimer’s

2260 N. Ridge Rd, Suite 240 Wichita, KS  67205 316-838-7700

AMR Norman is located in the heart of the Midwest – just minutes from Oklahoma City in Norman, Oklahoma. Previously Intend Research, this research center joined AMR officially in mid 2022. Lisa Connery, MD, has provided her medical experience as the site’s Principal Investigator since 2016.  AMR Norman has experience with anemia, chronic lower back pain, constipation, diabetes (Type I and Type II), fibromyalgia, hypertension and more. Our full-time research team includes clinical research coordinators, back-up coordinators, patient recruiters, lab coordinator, data entry coordinator, regulatory specialist, and administrative staff. We provide our community with innovative treatments and the highest quality of care throughout each clinical research trial.

1016 24th Ave., NW Suite 100 Norman, OK 73069 405-701-8999

Kansas City Oncology

AMR Kansas City Oncology has conducted 75 clinical trials. Recent experience includes Breast Cancer, Cancer Associated Pain, Carcinoma of unknown primary site, Colon Cancer, Esophageal Cancer, Hepatocellular Carcinoma (HCC), Immune Thrombocytopenia (ITP), Leukemia, Lung Cancer, Lymphoma, Melanoma, Myelodysplastic syndromes, Myeloma, Neuroendocrine Cancer, Prostate Cancer, Solid Tumors, Squamous Cell Carcinoma, and Pancreatic Cancer.

6740 Antioch Rd #101 Merriam, KS 66204 913-386-7556

801 North Weisgarber Rd, Suite 100 Knoxville, TN 37909 (615) 591-0211 [email protected]

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Researchers are working quickly to study COVID-19, its spread, prevention and treatment. With the world facing a pandemic, healthy volunteers and patients who have recovered from the virus are needed for clinical studies to help develop new vaccines and medications to fight the virus.

Eczema (Atopic Dermatitis)

Eczema is a common allergic skin condition that can cause a skin rash that is often itchy, red or scaly in appearance. Currently, there is no cure for eczema, and treatments focus on symptom management and trigger avoidance. Register with ICON to match with eczema research studies.

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Bullous pemphigoid is a rare skin condition most common in older adults. It can cause large fluid-filled blisters to form on the skin, often near joints and areas where the body bends, and may also cause mouth sores. Register with ICON to match with bullous pemphigoid studies.

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Scleroderma is a chronic, auto-immune disease that can cause scarring and damage to the skin and other organs. With no cure yet, current treatments may help relieve symptoms and slow disease progression. Register with ICON to match with scleroderma studies.

Hair loss, or alopecia, affects men and women and can have a profound effect on one's appearance and self-esteem. Causes include medical conditions, trauma and genetics. Register with ICON to match with alopecia studies.

Psoriasis is an auto-immune disease that causes skin cells to grow rapidly, creating raised plaques or scales on the body. There is no cure for psoriasis, but researchers continue to investigate new treatments. Register with ICON to match with psoriasis research studies.

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• News & Events
• Press releases

ICON to Acquire Clinical Research Management, Inc.

• Dublin, Ireland
• 13 February 2024

The acquisition extends ICON’s presence in government sponsored research and enhances capabilities in Vaccines and Infectious Disease

ICON plc, (NASDAQ: ICLR) a global provider of drug development solutions and services to the pharmaceutical, biotechnology and medical device industries, today announced that it has agreed, subject to certain customary closing conditions (including applicable regulatory approvals), to acquire Clinical Research Management, Inc. (ClinicalRM).

The acquisition will enhance ICON’s ability to access the market for government sponsored research and further enhances ICON’s capabilities in the areas of Vaccines and Infectious Disease.

ClinicalRM provide full service and functional research solutions to a broad range of US government agencies. Their extensive expertise extends across basic and applied research, infectious diseases, vaccines development and testing and the response to bio-threats. They have worked in collaboration with government and commercial customers to respond to the threat of global viral epidemics.

Commenting on the acquisition, ICON’s Chief Executive Officer, Ciaran Murray said: “The market for government sponsored research is significant with over fifteen hundred active clinical studies being funded by the National Institutes of Health or other federal agencies. ClinicalRM has strong relationships and a deep understanding of what is required to partner successfully with government sponsors. They will provide ICON a platform to further penetrate this market segment as part of our strategy to grow and diversify our customer base. ClinicalRM’s experience in responding to the challenges of global viruses will further enhance ICON’s capabilities in the areas of Vaccines and Infectious disease, benefiting our customers and patients globally.”

Victoria Tifft, Chief Executive Officer of ClinicalRM added, “ We are delighted to be joining ICON. By combining ClinicalRM’s expertise in government sponsored research with ICON’s breadth of services and global footprint we will be able to bring additional services and thought leadership to our customers. We are also excited about the potential the combination has to further innovate drug development in the area of Vaccines and Infectious diseases, important areas of focus for both government and commercial customers.”

About ClinicalRM

ClinicalRM is a full-service Contract Research Organisation specializing in preclinical through Phase IV support of clinical research and clinical trial services for biologics, drugs and devices. The organisation helps customers get their products to market faster with a wide array of research, regulatory and sponsor services within the U.S. and around the globe. From international partnerships and affiliations to government relations and local alliances, ClinicalRM delivers a synergy in the global market with projects spanning the government, academic and commercial marketplaces. The company has a distinct ability to provide boots-on-the-ground and rapid response efforts to global health crises.

About ICON plc

ICON plc is a global provider of drug development solutions and services to the pharmaceutical, biotechnology and medical device industries. The company specialises in the strategic development, management and analysis of programs that support clinical development - from compound selection to Phase I-IV clinical studies. With headquarters in Dublin, Ireland, ICON currently, operates from 89 locations in 37 countries and has approximately 12,200 employees. Further information is available at  www.iconplc.com .

ICON Media Contact

Niamh Murphy ICON +35312912180 [email protected]

This press release contains forward-looking statements. These statements are based on management's current expectations and information currently available, including current economic and industry conditions. These statements are not guarantees of future performance or actual results, and actual results, developments and business decisions may differ from those stated in this press release. The forward-looking statements are subject to future events, risks, uncertainties and other factors that could cause actual results to differ materially from those projected in the statements, including, but not limited to, the ability to enter into new contracts, maintain client relationships, manage the opening of new offices and offering of new services, the integration of new business mergers and acquisitions, as well as economic and global market conditions and other risks and uncertainties detailed from time to time in SEC reports filed by ICON, all of which are difficult to predict and some of which are beyond our control. For these reasons, you should not place undue reliance on these forward-looking statements when making investment decisions. The word "expected" and variations of such words and similar expressions are intended to identify forward-looking statements. Forward-looking statements are only as of the date they are made and we do not undertake any obligation to update publicly any forward-looking statement, either as a result of new information, future events or otherwise. More information about the risks and uncertainties relating to these forward-looking statements may be found in SEC reports filed by ICON, including its Form 20-F, F-1, S-8 and F-3, which are available on the SEC's website at  http://www.sec.gov .

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Sr Clinical Research Associate - Home-Based (St Louis/KC, USA)

• Location: Kansas City, St. Louis, United States
• Categories Clinical Monitoring
• __vacancyopjusttionswidget.opt-Business Area__ ICON Strategic Solutions
• __vacancyopjusttionswidget.opt-Remote Working __ Remote

About the role

This vacancy has now expired. please see similar roles below....

As a Sr. CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

General Summary

The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference on Harmonization Good Clinical Practices (ICH-GCP) and all applicable regulatory requirements.

Primary Responsibilities

• Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs, and study processes. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructions to site personnel and study close out.
• Verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations.
• Ensures the integrity of clinical data and that the study is conducted in compliance with the approved protocol, GCP, applicable regulations, and SOPs.
• Manages the investigative site staff to facilitate trial deliverables, e.g., subject enrollment, data deliverables.
• Verifies proper management and accountability of Investigational Product (IP).
• Writes and submits reports of investigational site findings and updates applicable tracking systems. Escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate.
• Manages essential documents as required by local regulations and ICH-GCP guidelines before, during, and after a clinical study; assists with resolution of investigational site/data queries.
• Performs key risk assessment and management responsibilities throughout the project, including key risk indicator and site health analysis, site process evaluation, and project escalation.
• Participates in audit preparation and follow-up activities as needed.

Level-Specific Responsibilities:

• Independently performs a variety of onsite and offsite monitoring visit types.
• Gathers and reviews information for assigned sites and identifies inconsistencies. With limited guidance from project and functional management, assesses risk and escalates as appropriate.
• Assists with non-complex ad hoc, short-term assignments in support of additional studies or departmental initiatives.
• May serve as preceptor, providing training to less experienced clinical team members

Qualifications:

• Equivalent combination of education, training and relevant experience may be considered in place of the education and experience stated above. All employees must read, write and speak fluent English and host country language.
• 4 years of experience supporting clinical trials including 3 years of on-site monitoring experience
• In-depth knowledge of the drug development process
• In-depth knowledge and practical utilization of ICH- GCP and applicable regulatory requirements
• Sound knowledge of applicable policies and procedures, SOPs, work instructions and other guidance documents
• Good spoken and written communication skills; good presentation skills
• Strong interpersonal, collaboration and time management skills
• High proficiency with Microsoft Office and company collaboration applications
• Excellent skill in the utilization of applicable clinical systems
• Excellent critical thinking skills
• Excellent organizational skills
• Ability to focus on detail for extended periods of time; high attention to accuracy
• Ability to travel extensively
• Ability to establish and maintain effective working relationships with investigative site staff

Why ICON? Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development. ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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